食品研究与开发
食品研究與開髮
식품연구여개발
FOOD RESEARCH AND CEVELOPMENT
2014年
21期
70-73
,共4页
曹志海%王伟萍%张宣伟%陈笑笑%桑丽雅%胡叶军
曹誌海%王偉萍%張宣偉%陳笑笑%桑麗雅%鬍葉軍
조지해%왕위평%장선위%진소소%상려아%호협군
硝基呋喃类代谢物%水产品%胶体金%样品前处理
硝基呋喃類代謝物%水產品%膠體金%樣品前處理
초기부남류대사물%수산품%효체금%양품전처리
nitrofuran metabolites%aquatic products%colloidal gold%sample pretreatment
采用胶体金免疫层析方法建立了水产品中硝基呋喃类代谢物的快速检测,并对其样品前处理方法进行了研究。结果表明,最佳衍生剂为4-硝基苯甲醛(4-NP),用量为0.1 mL,衍生条件为60℃水浴条件下孵育60 min,提取剂用量为6.0 mL,净化剂用量为1.0 mL。呋喃唑酮代谢物(AOZ)、呋喃西林代谢物(SEM)、呋喃它酮代谢物(AMOZ)、呋喃妥因代谢物(AHD)的线性范围分别为0.0μg/L~4.0μg/L、0.0μg/L~4.0μg/L、0.0μg/L~6.0μg/L、0.0μg/L~6.0μg/L;添标回收率均为76.6%~102.3%;相对标准偏差均为3.03%~7.40%。该样本前处理方法适合硝基呋喃类代谢物免疫胶体金快速检测。
採用膠體金免疫層析方法建立瞭水產品中硝基呋喃類代謝物的快速檢測,併對其樣品前處理方法進行瞭研究。結果錶明,最佳衍生劑為4-硝基苯甲醛(4-NP),用量為0.1 mL,衍生條件為60℃水浴條件下孵育60 min,提取劑用量為6.0 mL,淨化劑用量為1.0 mL。呋喃唑酮代謝物(AOZ)、呋喃西林代謝物(SEM)、呋喃它酮代謝物(AMOZ)、呋喃妥因代謝物(AHD)的線性範圍分彆為0.0μg/L~4.0μg/L、0.0μg/L~4.0μg/L、0.0μg/L~6.0μg/L、0.0μg/L~6.0μg/L;添標迴收率均為76.6%~102.3%;相對標準偏差均為3.03%~7.40%。該樣本前處理方法適閤硝基呋喃類代謝物免疫膠體金快速檢測。
채용효체금면역층석방법건립료수산품중초기부남류대사물적쾌속검측,병대기양품전처리방법진행료연구。결과표명,최가연생제위4-초기분갑철(4-NP),용량위0.1 mL,연생조건위60℃수욕조건하부육60 min,제취제용량위6.0 mL,정화제용량위1.0 mL。부남서동대사물(AOZ)、부남서림대사물(SEM)、부남타동대사물(AMOZ)、부남타인대사물(AHD)적선성범위분별위0.0μg/L~4.0μg/L、0.0μg/L~4.0μg/L、0.0μg/L~6.0μg/L、0.0μg/L~6.0μg/L;첨표회수솔균위76.6%~102.3%;상대표준편차균위3.03%~7.40%。해양본전처리방법괄합초기부남류대사물면역효체금쾌속검측。
Based on colloidal gold immunochromatography assay to detect the content of nitrofuran metabolites in aquatic products, and study on sample pretreatment. The results showed that the best derivatizing agent was 4-nitrobenzaldehyde (4-NP), dosage was 0.1 mL. Derivative conditions was 60℃water bath conditions incubated for 60 min.The dosage of extractant and purifying agent were 6.0 and 1.0 mL. The linear range of AOZ,SEM, AMOZ,AHD were 0.0μg/L-4.0μg/L,0.0μg/L-4.0μg/L,0.0μg/L-4.0μg/L,0.0μg/L-4.0μg/L. The recovery rate and the relative standard deviation were 76.6%-102.3%and 3.03%-7.40%. This sample pre-treatment method was suitable for the the nitrofuran metabolites immune colloidal gold rapid detection.